A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913867



Internal ID22689083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69710239..69711706hg38UCSC Ensembl
chr9:72325155..72326622hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381468
hg191468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432293
Samples
Known GenesPTAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913867
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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